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Journal Abstract Search

318 related items for PubMed ID: 2286031

  • 1. Duchenne and Becker muscular dystrophies: genetics, prenatal diagnosis, and future prospects.
    Bieber FR, Hoffman EP.
    Clin Perinatol; 1990 Dec; 17(4):845-65. PubMed ID: 2286031
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  • 2. Gene-deletion and carrier detections, and prenatal diagnosis of Duchenne muscular dystrophy by analysis of the dystrophin gene amplified by polymerase chain reaction.
    Fujishita S, Shibuya N, Niikawa N, Nagataki S.
    Jinrui Idengaku Zasshi; 1991 Dec; 36(4):317-24. PubMed ID: 1811098
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  • 3. In utero fetal muscle biopsy alters diagnosis and carrier risks in Duchenne and Becker muscular dystrophy.
    Evans MI, Krivchenia EL, Johnson MP, Quintero RA, King M, Pegoraro E, Hoffman EP.
    Fetal Diagn Ther; 1995 Dec; 10(2):71-5. PubMed ID: 7794517
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  • 4. Dystrophin analysis in duchenne muscular dystrophy: use in fetal diagnosis and in genetic counseling.
    Bieber FR, Hoffman EP, Amos JA.
    Am J Hum Genet; 1989 Sep; 45(3):362-7. PubMed ID: 2672800
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  • 5. Prenatal diagnosis of Duchenne muscular dystrophy: prospective linkage analysis and retrospective dystrophin cDNA analysis.
    Ward PA, Hejtmancik JF, Witkowski JA, Baumbach LL, Gunnell S, Speer J, Hawley P, Tantravahi U, Caskey CT.
    Am J Hum Genet; 1989 Feb; 44(2):270-81. PubMed ID: 2643315
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  • 8. Dystrophinopathies.
    Reitter B, Goebel HH.
    Semin Pediatr Neurol; 1996 Jun; 3(2):99-109. PubMed ID: 8795844
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  • 11. Relatively low proportion of dystrophin gene deletions in Israeli Duchenne and Becker muscular dystrophy patients.
    Shomrat R, Gluck E, Legum C, Shiloh Y.
    Am J Med Genet; 1994 Feb 15; 49(4):369-73. PubMed ID: 8160727
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  • 13. Experience and strategy for the molecular testing of Duchenne muscular dystrophy.
    Prior TW, Bridgeman SJ.
    J Mol Diagn; 2005 Aug 15; 7(3):317-26. PubMed ID: 16049303
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  • 14. Prediction of dystrophin phenotype by DNA analysis in Duchenne/Becker muscular dystrophy.
    Specht LA, Beggs AH, Korf B, Kunkel LM, Shapiro F.
    Pediatr Neurol; 1992 Aug 15; 8(6):432-6. PubMed ID: 1476571
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  • 16. Fluorescent multiplex linkage analysis and carrier detection for Duchenne/Becker muscular dystrophy.
    Schwartz LS, Tarleton J, Popovich B, Seltzer WK, Hoffman EP.
    Am J Hum Genet; 1992 Oct 15; 51(4):721-9. PubMed ID: 1415217
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  • 19. [Deletions within the gene of dystrophin in Duchenne and Becker muscular dystrophy].
    Zimowski JG, Bisko M, Fidziańska E, Hausmanowa-Petrusewicz I, Badurska B, Borkowska J, Lusakowska A, Fidziańska A, Jezuita J, Zaremba J.
    Neurol Neurochir Pol; 1993 Oct 15; 27(4):469-78. PubMed ID: 8247234
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  • 20. [Molecular genetics of Duchenne/Becker muscular dystrophy].
    Saito K, Ikeya K, Kondo E, Yamauchi A, Komine S, Fukuyama Y.
    Nihon Rinsho; 1993 Sep 15; 51(9):2420-7. PubMed ID: 8411723
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